Total Carbohydrate Assay (ab155891) is a simple, sensitive and robust method of detecting virtually all carbohydrates.
Colorimetric
Tissue, Suspension cells, Tissue Extracts, Adherent cells
Quantitative
30m
Total Carbohydrate Assay (ab155891) is a simple, sensitive and robust method of detecting virtually all carbohydrates.
Colorimetric
Tissue, Suspension cells, Tissue Extracts, Adherent cells
Quantitative
30m
Microplate reader
Blue Ice
+4°C
+4°C
+4°C
Total Carbohydrate Assay (ab155891) is a simple, sensitive and robust method of detecting virtually all carbohydrates.
The carbohydrate assay protocol is based on the phenol - sulfuric acid assay. In the assay, polysaccharides (mono, di, tri, etc.) and their derivatives, in the presence of sulfuric acid, are hydrolyzed to monomers and converted to furfural or hydroxyfurfural. These react with the developer to form a chromogen that can be quantified by measuring the absorbance at λ = 490 nm.
The total carbohydrate assay kit can detect most forms of carbohydrates, including simple and complex saccharides, glycans, glycoproteins and glycolipids.
Total carbohydrate assay protocol summary:
- add samples and glucose standards to wells
- add concentrated sulfuric acid and incubate for 15 min at 90°C
- add developer and incubate for 5 min
- analyze with a microplate reader
This product is manufactured by BioVision, an Abcam company and was previously called K645 Total Carbohydrate Colorimetric Assay Kit. K645-100 is the same size as the 100 test size of ab155891.
Carbohydrates play important structural as well as chemical roles in all living systems. Detection of total carbohydrates, therefore, has wide applications.
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Full details and terms and conditions can be found here:
Terms & Conditions.
Carbohydrates in food items and mouse tissue lysates, shown as mg per mg of extracted protein (duplicates; +/- SD).
Carbohydrates measured in orange juice and caster sugar. Background signal subtracted, duplicates; +/- SD.
Carbohydrates from lysed non-differentiated or adipose differentiated 3T3L1 cells (duplicates; +/- SD). Cells were differentiated using a mixture of small molecules: IBMX, Non-specific cAMP and cGMP inhibitor ab120840, Dexamethasone, anti-inflammatory glucocorticoid ab120743 and Recombinant human Insulin protein (Active) ab123768.
D-Glucose standard curve generated using the method described in the protocol bookelt.
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